Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
---|---|
Alliance of Genome Resources | July 29, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
---|---|---|---|---|---|---|---|---|
DOID:4362 | cervical cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
DOID:3307 | teratoma | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
DOID:0111953 | immunodeficiency 23 | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
DOID:162 | cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
DOID:0050161 | lower respiratory tract disease | FB:FBgn0035976 | Drosophila melanogaster (fruit fly) | 39063 | PGRP-LC | CG4432 |
|
|
DOID:0050161 | lower respiratory tract disease | FB:FBgn0030695 | Drosophila melanogaster (fruit fly) | 32534 | PGRP-LE | CG8995 |
|
|
DOID:2747 | glycogen storage disease | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
DOID:1459 | hypothyroidism | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
DOID:0050545 | visceral heterotaxy | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
DOID:0111042 | glycogen storage disease IXa | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
DOID:2747 | glycogen storage disease | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
DOID:0111041 | glycogen storage disease IXb | HGNC:8927 | Homo sapiens (human) | 5257 | PHKB |
|
||
DOID:5082 | liver cirrhosis | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
|
||
DOID:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
|
||
DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
|
||
DOID:0112347 | hereditary spastic paraplegia 84 | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
|
||
DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
|
||
DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:8984 | Homo sapiens (human) | 5298 | PI4KB |
|
||
DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
|
||
DOID:0060284 | paroxysmal nocturnal hemoglobinuria | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
|
||
DOID:0060713 | autosomal recessive congenital ichthyosis 4B | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
|
||
DOID:0112216 | developmental and epileptic encephalopathy 80 | FB:FBgn0035464 | Drosophila melanogaster (fruit fly) | 38446 | PIG-B |
|
||
DOID:10112 | sleeping sickness | FB:FBgn0035464 | Drosophila melanogaster (fruit fly) | 38446 | PIG-B |
|
||
DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | FB:FBgn0265174 | Drosophila melanogaster (fruit fly) | 19835383 | PIG-V |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024